Implantable heart assist system and method of applying same

ABSTRACT

An extracardiac pumping for supplementing the circulation of blood, including the cardiac output, in a patient without any component thereof being connected to the patient&#39;s heart, and methods of using same. One embodiment provides a vascular graft that has a first end that is sized and configured to couple to a non-primary blood vessel and a second end that is fluidly coupled to a pump to conduct blood between the pump and the non-primary blood vessel. An outflow conduit is also provided that has a first end sized and configured to be positioned within the same or different blood vessel, whether primary or non-primary, through the vascular graft. The outflow conduit is fluidly coupled to the pump to conduct blood between the pump and the patient. The vascular graft may be connected to the blood vessel subcutaneously to permit application of the extracardiac pumping system in a minimally-invasive procedure.

RELATED APPLICATIONS

This application is a continuation of U.S. Application No. 10/289,467,filed Nov. 6, 2002, now U.S. Pat. No. 6,889,082, which is acontinuation-in-part of U.S. application Ser. No. 10/171,023, filed onJun. 11, 2002, now U.S. Pat. No. 6,685,621 which is acontinuation-in-part of U.S. application Ser. No. 10/078,260, filed onFeb. 15, 2002 now U.S. Pat. No. 6,610,004, which is acontinuation-in-part of U.S. application Ser. No. 09/552,979, filed onApr. 21, 2000, now U.S. Pat. No. 6,390,969 B1, which is acontinuation-in-part of U.S. application Ser. No. 09/470,841, filed onDec. 23, 1999, now U.S. Pat. No. 6,387,037 B1, which is acontinuation-in-part of U.S. application Ser. No. 09/289,231, filed onApr. 9, 1999, now U.S. Pat. No. 6,428,464 B1, which iscontinuation-in-part of U.S. application Ser. No. 09/166,005, filed onOct. 2, 1998, now U.S. Pat. No. 6,200,260 B1, which claims the benefitof U.S. Provisional Application Ser. No. 60/061,434, filed Oct. 9, 1997,all of which are hereby expressly incorporated by reference herein intheir entirety.

FIELD OF THE INVENTION

The present invention relates generally to a system for assisting theheart and, in particular, to an extracardiac pumping'system and a methodfor both supplementing the circulation of blood through the patient andfor enhancing vascular blood mixing using a minimally invasiveprocedure.

BACKGROUND OF THE INVENTION

During the last decade, congestive heart failure (CHF) has burgeonedinto the most important public health problem in cardiovascularmedicine. As reported in Gilum, R. F., Epidemiology of Heart Failure inthe U.S., 126 Am. Heart J. 1042 (1993), four hundred thousand (400,000)new cases of CHF are diagnosed in the United States annually. Thedisorder is said to affect nearly 5 million people in this country andclose to 20 million people worldwide. The number of hospitalizations forCHF has increased more than three fold in the last 15 years.Unfortunately, nearly 250,000 patients die of heart failure annually.According to the Framingham Heart Study, the 5-year mortality rate forpatients with congestive heart failure was 75 per cent in men and 62 percent in women (Ho, K. K. L., Anderson, K. M., Kannel, W. B., et al.,Survival After the Onset of Congestive Heart Failure in Framingham HeartStudy Subject, 88 Circulation 107 (1993)). This disorder represents themost common discharge diagnosis for patients over 65 years of age.Although the incidence of most cardiovascular disorders has decreasedover the past 10 to 20 years, the incidence and prevalence of congestiveheart failure has increased at a dramatic rate. This number willincrease as patients who would normally die of an acute myocardialinfarction (heart attack) survive, and as the population ages.

CHF manifests itself primarily by exertional dyspnea (difficult orlabored breathing) and fatigue. Three paradigms are used to describe thecauses and therapy of CHF. The first views this condition in terms ofaltered pump function and abnormal circulatory dynamics. Other modelsdescribe it largely in terms of altered myocardial cellular performanceor of altered gene expression in the cells of the atrophied heart. Inits broadest sense, CHF can be defined as the inability of the heart topump blood throughout the body at the rate needed to maintain adequateblood flow, and many of the normal functions of the body.

To address CHF, many types of cardiac assist devices have beendeveloped. A cardiac or circulatory assist device is one that aids thefailing heart by increasing its pumping function or by allowing it acertain amount of rest to recover its pumping function. Becausecongestive heart failure may be chronic or acute, different categoriesof heart assist devices exist. Short of a heart transplant, at least twotypes of chronic heart assist systems have been developed. One typeemploys a full or partial prosthetic connected between the heart and theaorta, one example of which is commonly referred to as a LVAD—LeftVentricular Assist Device. With reference to FIG. 1 herein, one exampleof a LVAD 2 is shown. The LVAD comprises a pump and associated valves 4that draws blood directly from the apex of the left ventricle 6 anddirects the blood to the aortic arch 8, bypassing the aortic valve. Inthis application, the left ventricle stops functioning and does notcontract or expand. The left ventricle becomes, in effect, an extensionof the left atrium, with the LVAD 2 taking over for the left ventricle.The ventricle, thus, becomes a low-pressure chamber. Because the intentis to take over for the left ventricle, the LVAD operates by pumpingblood at cardiac rates. With an LVAD, oxygenated blood circulation isestablished sufficient to satisfy the demand of the patient's organs.Under these circumstances, however, continuous flow may not be desiredbecause the patient's arterial system is deprived of pulsatile waveflow, which is beneficial to certain parts of the patient.

Another type of chronic heart assist system is shown in U.S. Pat. No.5,267,940 to Moulder. Moulder describes a pump implanted into theproximal descending aorta to assist in the circulation of blood throughthe aorta. Because it is intended to pump blood flowing directly out ofthe heart, it is important that the Moulder device operate in a properlytimed, pulsatile fashion. If it is not operated in directsynchronization with the patient's heart, there is a risk that the pumpmight cause “carotid steal phenomenon” where blood is drawn away fromthe patient's brain through the carotid arteries when there isinsufficient blood in the left ventricle.

In addressing acute CHF, two types of heart assist devices have beenused. One is counterpulsatory in nature and is exemplified by anintra-aortic balloon pump (IABP). With an IABP, the balloon is collapsedduring isovolumic contraction, providing a reduced pressure againstwhich the heart must pump blood, thereby reducing the load on the heartduring systole. The balloon is then expanded, forcing bloodomnidirectionally through the arterial system. Another example of thisfirst type employs one or more collapsible chambers in which blood flowspassively into the chamber during systole, as is shown in U.S. Pat. No.4,240,409 to Robinson et al. The chamber is then collapsed and the bloodforcibly returned to the aorta. These devices simulate a chamber of theheart and depend upon an inflatable bladder to effectuate pumpingaction, requiring an external pneumatic driver. Moreover, they do notoperate as a continuous flow system, operating exclusively in pulsatilefashion.

A second type of acute assist device utilizes an extracorporeal pump,such as the Biomedicus centrifugal pump, to direct blood through thepatient while surgery is performed on the heart. In one example,described in U.S. Pat. No. 4,968,293 to Nelson, the heart assist systememploys a centrifugal pump in which the muscle of the patient isutilized to add pulsatility to the blood flow. The Nelson device is usedto bypass a portion of the descending aorta.

Another device, shown in U.S. Pat. No. 4,080,958 to Bregman et al.,utilizes an inflatable and collapsible bladder to assist in bloodperfusion during heart trauma and is intended to supplement aconventional heart-lung machine by imparting pulsatile actuation. In theprimary embodiment disclosed in Bregman, the balloon is controlled tomaintain sufficient pressure at the aortic root during diastole toensure sufficient blood perfusion to the coronary arteries. In analternative embodiment, a low resistance outlet from the aorta to theinferior vena cava is provided to reduce the aortic pressure duringsystole, thus, reducing the hemodynamic load on the left ventricle.

Other devices, such as that shown in U.S. Pat. No. 4,034,742 to Thoma,depend upon interaction and coordination with a mechanical pumpingchamber containing a movable pumping diaphragm. These devices areintended primarily for application proximate the heart and within thepatient's thorax, requiring major invasive surgery.

Many CHF devices are acutely used in the perioperative period. Forexample, U.S. Pat. No. 4,995,857 to Arnold discloses a perioperativedevice to pump blood at essentially cardiac rates during surgery whenthe heart has failed or has been stopped to perform cardiac surgery. TheArnold system temporarily replaces the patient's heart and lung andpumps blood at cardiac rates, typically 5 to 6 liters/min. Like allsystems that bypass the heart and the lungs, an oxygenator is required.Of course, with any system that includes an oxygenator, such as theconventional heart-lung machine, the patient cannot be ambulatory.

With early IABP devices, a polyurethane balloon was mounted on avascular catheter, inserted into the femoral artery, and positioned inthe descending aorta just distal to the left subclavian artery. Theballoon catheter was connected to a pump console that pumped helium orcarbon dioxide into the balloon during diastole to inflate it. Duringisovolumic contraction, i. e., during the brief time that the aorticvalve is closed and the left ventricle continues to contract, the gasused to actuate the balloon was rapidly withdrawn to deflate theballoon. This reduced the pressure at the aortic root when the aorticvalve opened. In contrast, during diastole, the balloon was inflated,causing the diastolic pressure to rise and pushing the blood in theaorta distally towards the lower part of the body (on one side of theballoon) and proximally toward the heart and into the coronary arteries(on the other).

The major advantage in such a counterpulsation device was systolicdeflation, which lowered the intra-aortic volume and pressure, reducingboth afterload and myocardial oxygen consumption. In other words, whenthe balloon is inflated, it creates an artificially higher pressure inthe aorta, which has the ancillary benefit of greater perfusion throughthe coronary arteries. When the balloon deflates, just before the aorticvalve opens, the pressure and volume of the aorta decrease, relievingsome of the hemodynamic burden on the heart. These physiologic responsesimproved the patient's cardiac output and coronary circulation,temporarily improving hemodynamics. In general, counterpulsation with anIABP can augment cardiac output by about 15%, this being frequentlysufficient to stabilize the patient's hemodynamic status, which mightotherwise rapidly deteriorate. When there is evidence of more efficientpumping ability by the heart, and the patient has moved to an improvedclass of hemodynamic status, counterpulsation can be discontinued, byslowly weaning while monitoring for deterioration.

Until 1979, all IABP catheters were inserted via surgical cutdown,generally of the femoral artery. Since then, the development of apercutaneous IABP catheter has allowed quicker, and perhaps safer,insertion and has resulted in more expeditious institution of therapyand expansion of clinical applications. Inflation and deflation of theballoon, however, requires a pneumatic pump that is sufficiently largethat it must be employed extracorporeally, thereby restricting thepatient's movements and ability to carry out normal, daily activities.IABP devices are, thus, limited to short term use, on the order of a fewdays to a few weeks.

As discussed above, a variety of ventricular assist pumping mechanismshave been designed. Typically associated with LVADs are valves that areused in the inlet and outlet conduits to insure unidirectional bloodflow. Given the close proximity of the heart, unidirectional flow wasnecessary to avoid inadvertent backflow into the heart. The use of suchvalves also minimized the thrombogenic potential of the LVAD device.

Typically, the pump associated with older LVADs was a bulky pulsatileflow pump, of the pusher plate or diaphragm style, such as thosemanufactured by Baxter Novacor or TCI, respectively. Given that the pumpwas implanted within the chest and/or abdominal cavity, major invasivesurgery was required. The pumps were typically driven through apercutaneous driveline by a portable external console that monitors andreprograms functions.

Alternatively, rotary pumps, such as centrifugal or axial pumps, havebeen used in heart assist systems. With centrifugal pumps, the bloodenters and exits the pump practically in the same plane. An axial pump,in contrast, directs the blood along the axis of rotation of the rotor.Inspired by the Archimedes screw, one design of an axial pump has beenminiaturized to about the size of a pencil eraser, although otherdesigns are larger. Despite its small size, an axial pump may besufficiently powerful to produce flows that approach those used witholder LVADs. Even with miniaturized pumps, however, the pump istypically introduced into the left-ventricle through the aortic valve orthrough the apex of the heart, and its function must be controlled froma console outside the body through percutaneous lines.

All of these heart assist systems referred to above serve one or both oftwo objectives: (1) to improve the performance of a patient'soperative-but-diseased heart from the minimum, classified as NYHAC ClassIV, to practically normal, classified as I or 0; or (2) to supplementoxygenated blood circulation through the patient to satisfy organ demandwhen the patient's heart is suffering from CHF. With such systems,extreme pumping and large amounts of energy, volume, and heatdissipation are required.

Many of these heart assist systems have several general features incommon: 1) the devices are cardiac in nature; i. e., they are placeddirectly within or adjacent to the heart, or within one of the primaryvessels associated with the heart (aorta), and are often attached to theheart and/or aorta; 2) the devices attempt to reproduce pulsatile bloodflow naturally found in the mammalian circulatory system and, therefore,require valves to prevent backflow; 3) the devices are driven fromexternal consoles, often triggered by the electrocardiogram of thepatient; and 4) the size of the blood pump, including its associatedconnectors and accessories, is generally unmanageable within the anatomyand physiology of the recipient. Due to having one or more of thesefeatures, the prior art heart assist devices are limited in theireffectiveness and/or practicality.

Many of the above identified prior art systems, generally referred to asMechanical Circulatory Assist Devices, are not the only means, however,used to treat patients with congestive heart failure (CHF). Most CHFpatients are prescribed as many as five to seven different drugs toameliorate their signs and symptoms. These drugs may include diuretics,angiotensin converting enzyme (ACE) inhibitors, beta-blockers, cardiacglycosides, and peripheral vasodilators. The rationale forpharmacological intervention in heart failure include minimizing theload on the heart, improving the pumping action of the heart byenhancing the contractility of the muscle fibers, and suppression ofharmful neurohormonal compensatory mechanisms that are activated becauseof the decreased pumping function of the heart.

Noncompliance with what is often a complex drug regime may dramaticallyadversely affect the recovery of a CHF patient leading to the need forhospitalization and possibly morbidity and mortality. In addition, ACEinhibitors and diurectics can cause hypotension, which leads todecreased organ perfusion or an increasing demand on the heart to pumpmore blood. This leads to an inability, in many cases, to prescribe themost effective dosage of ACE inhibitors and a less than optimum outcomefor the patient. Patients suffering from CHF with the underlying causeof mitral valve insufficiency have been able to have their diureticsreduced following surgical repair of their mitral valve. This is due toan increased cardiac output and arterial pressures (as a result of thecorrection of the problem) resulting in more effective organ perfusion.With the reduction in the use of diuretics and the resultanthypotension, more effective dosages of ACE inhibitors can be used withmore favorable outcomes. In addition, it is easier for the patient tofollow a less complex drug regime, eliminating the costly and lifethreatening risks associated with noncompliance.

When blood flow through the coronary arteries falls below the levelneeded to provide the energy necessary to maintain myocardial function,due often to a blockage in the coronary arteries, a myocardialinfarction or heart attack occurs. This is a result of the blockage inthe coronary arteries preventing blood from delivering oxygen to tissuesdownstream of the blockage. The closer the blockage is to the coronaryostia, however, the more severe and life threatening the myocardialinfarction. The farther the location of the blockage is from thecoronary ostia, the smaller the area of tissue or myocardium that is atrisk. As the energy stored in the affected area decreases, myocardialcells begin to die. The larger the area that dies due to the loss ofoxygen, the more devastating the infarction. To reduce the area at risk,at least two known options are to either increase the oxygen supply tothe affected area or decrease the energy demands of the heart to prolongenergy stores until the blockage can be removed or reduced. Oneparticular method to increase blood flow, thereby increasing delivery ofoxygen to the affected area, is through a technique calledretroperfusion. This is accomplished by passing a cannula into eitherthe right or left ventricle (depending on the area of the blockage) andperfusing oxygenated blood retrograde up the coronary artery on thedownstream side of the blockage. Another method is to use drugs toincrease the force of contraction of the myocardium, creating increasedblood flow across the blocked area. Yet another method is to use drugs,such as pentoxifylline, aspirin, or TPA (tissue plaminogen activator),to reduce the viscosity of (thin out) the blood, inhibit plateletaggregation, or lyse thrombi (clots), respectively, thus, allowing moreblood to pass by the blockage. The goal of all of these methods is toincrease the delivery of oxygen to the tissue at risk.

The alternative option mentioned above is to reduce the energy demandsof the myocardium and increase the amount of time before irreversibledamage occurs. This can be accomplished by reducing the workload of theleft ventricle (which is the largest energy-consuming portion of theheart). An IABP is placed into the aorta and used as described above,resulting in a decreased afterload on the heart and increased perfusionof the coronary arteries and peripheral organs. An alternative way toreduce myocardial oxygen demand is to reduce the volume of blood theleft ventricle must pump. This can be accomplished by reducing the loadon the left ventricle, such as in a cardiopulmonary bypass or use of anLVAD. Unloading the left ventricle decreases the energy requirements ofthe myocardium and increases the amount of time before irreversibledamage occurs. This provides an opportunity to more effectively removeor decrease the blockage and salvage myocardial function. To besuccessful, each of these techniques must be implemented within a shortamount of time after the onset of a myocardial infarction. Thedisadvantage, however, is that each of these techniques can only beperformed in an emergency room or hospital setting. Unless the patientis already in the hospital when the myocardial infarction occurs, thereis usually some level of irreversible damage and subsequent loss ofmyocardial function.

There are yet other means of addressing and treating congestive heartfailure and related valvular disorders that involve the application ofshape change therapies. Those therapies including the use of one or morecardiac reshaping devices designed to squeeze an enlarged heart, or atleast an enlarged ventricle within the heart, in an to attempt torestore the heart to its normal healthy size. Such therapy is alsodesigned to maintain the ventricle and/or heart at that normal sizewhile the underlying problem is addressed. By doing so, the therapyresults in controlling the physical strain placed on the myocardiumcaused by a weakened heart and/or a defective heart valve. Such devicesare described, for example, in U.S. Pat. No. 6,085,754 to Alferness etal., which discloses a jacket of biological compatible material intendedto be placed over the apex of the heart. According to the '754 patent,the heart assumes a maximum adjusted volume for the jacket to constraincircumferential expansion of the heart beyond the maximum adjustedvolume during diastole and to permit unimpeded contraction of the heartduring systole. Another example is described in U.S. Pat. No. 6,224,540to Lederman et al., which discloses a passive girdle wrapped around aheart muscle that has dilatation of a ventricle to conform to the sizeand shape of the heart and to constrain the dilatation during diastole.Other examples are shown in U.S. Pat. No. 6,183,411 to Mortier et al.,which discloses alternative configurations including bands, frames andsocks and other apparatus formed to fit around an ailing heart to reduceheart wall stress, and in U.S. Pat. Nos. 6,221,103 and 6,190,408, whicheach disclose a device for restructuring heart chamber geometry. Whilethere may be advantages to using such devices to treat congestive heartfailure, there is the disadvantage that it is difficult to determine howfar to squeeze the ventricle and/or heart to restore it to its normalsize. Moreover, the heart walls are already stressed and enlarged uponthe application of such devices. A process of reducing the stress on theheart walls and, thus, the size of the ventricles, prior to applying arestricting device to minimize enlargement during the healing processwould be advantageous.

It would be advantageous, therefore, to employ a heart assist systemthat avoids major invasive surgery and also avoids the use of peripheralequipment that severely restricts a patient's movement. It would also beadvantageous to have such a heart assist system that can be employed ina non-hospital setting for ease of treating acute heart problems underemergency conditions. Yet another advantage would be to employ a processof reducing the size of the ventricle and/or the heart, and at the sametime the load on the heart, prior to applying a cardiac reshapingdevice.

SUMMARY OF THE INVENTION

The object of the present invention is to address the aspect of CHF thatresults from altered pump function and abnormal circulatory dynamicswhile overcoming the limitations of prior art heart assist systems.Without functioning as a bypass to one or more of a patient's organs,the present invention comprises an extracardiac pumping system forsupplementing the circulation of blood through the patient without anycomponent thereof being connected to the patient's heart or primaryvessels. Thus, it is extracardiac in nature. With the ability to beapplied within a minimally invasive procedure, the present inventionsignificantly improves the condition of the patient suffering from CHF,resulting in the patient feeling much better, even where CHF continues.By supplementing the pumping action of the heart, in lieu of replacingit, the various embodiments of the present invention take advantage ofthe pulsatile action of the heart, despite its weakened condition, toeffectively deliver blood to body organs that benefit from pulsatiledelivery of oxygenated blood. As a result, the present invention iscapable of being operated in a continuous flow fashion or, if desired,in a pulsatile flow fashion.

An ancillary but important benefit of the present invention is theability to apply the present invention in such a way as to also reducethe pumping load on the heart and/or to reduce ventricular loading,thereby potentially permitting the heart to recover during use. With thepresent invention, no bulky pump, valves or oxygenator are required, andno thoracic invasion with major cardiac surgery is required. Indeed, asignificant advantage of the present invention is its simplicity whileachieving extraordinary results in improving the condition of a patientsuffering from CHF. It is contemplated that the present invention beapplied such that the heart experiences a reduced pressure at the aorticroot during systole (afterload) and/or a reduced left ventricular enddiastolic pressure (pre-load), thus reducing the hemodynamic burden orworkload on the heart and, thus, permitting the heart to recover. Theresult is that the present systems and methods described herein have thebenefit of reducing ventricular loading.

The extracardiac system of the present invention preferably comprises,in several embodiments, a rotary pump configured to pump blood throughthe patient at subcardiac rates; i. e., at a flow rate significantlybelow that of the patient's heart. Other types of pumps or flowgenerating mechanisms may be effective as well, including but notlimited to rotating means, e.g., an Archimedes screw or impeller housedwithin an open or closed housing, either of which may be cable driven orshaft driven. Pumping the blood tends to revitalize the blood to acertain extent by imparting kinetic and potential energy to the blooddischarged from the pump. Importantly, the preferred pump for thepresent invention pumping system is one that requires a relatively lowamount of energy input, when compared to prior art pumps designed topump at cardiac rates. The pump may be implanted corporeally or morespecifically intravascularly, or it may be positioned extracorporeally,depending upon the capability, practicality, or need of the patient tobe ambulatory.

The present invention also comprises, in several embodiments, an inflowconduit fluidly coupled to the pump, to direct blood to the pump from afirst blood vessel, either the aorta or a first peripheral ornon-primary vessel, either directly or indirectly through another bloodvessel, wherein insertion of the pump and/or inflow conduit is through anon-primary blood vessel. The invention further comprises an outflowconduit fluidly coupled to the pump, to direct blood from the pump to asecond blood vessel, either the aorta or a second peripheral ornon-primary blood vessel, whether directly to the second vessel orindirectly through the first or other peripheral or non-primary bloodvessel. The connection and/or coupling of the inflow and outflowconduits to the respective blood vessels is performed subcutaneously;not so deep as to involve major invasive surgery. In other words,minimally subdermal. This permits application of the connections in aminimally-invasive procedure. Preferably, the connections to the bloodvessels are just below the skin or just below the first layer of muscle,depending upon the blood vessels at issue or the location of theconnection, although slightly deeper penetrations may be necessary forsome patients or for some applications.

In one embodiment, the present invention is configured so that it may beapplied at a single cannulated site and comprises, for example, amulti-lumen catheter having at least one lumen as an inflow lumen and asecond lumen as an outlet lumen. The multi-lumen catheter has an inflowport in fluid communication with the inflow lumen. With this embodiment,blood may be drawn into the inflow port of the first lumen from a firstperipheral or non-primary blood vessel site, either the blood vesselinto which the multi-lumen catheter is inserted or a different bloodvessel. The output of the pump directs blood through a second (outlet)port at the distal end of the second lumen that may be located in asecond peripheral or non-primary vessel site. This method accomplishesthe same beneficial results achieved in the previously describedembodiments, but requires only a single cannulated site, rather than twosuch sites. It should be appreciated that the multi-lumen catheter couldbe used in a manner where the outflow of the cannula is directed to thefirst vessel, while the inflow is drawn from the second vessel. Furtherstill, it should be appreciated that in one application the inflow lumencould be positioned to draw blood from a peripheral or non-primaryvessel at the site of entry into the patient while the outflow could bepositioned in the aorta, proximate an arterial branch.

The pump of the present invention may be a continuous flow pump, apulsatile pump, and/or a hybrid pump that is configured to generate flowin both a continuous and pulsatile format. The pump may be implantableand is used to fluidly connect two blood vessels, such as the femoralartery at the inflow and the left axillary artery at the outflow,although other peripheral or non-primary arterial and venous bloodvessels are contemplated, as well as any singular and/or cumulativecombination thereof. An alternative embodiment employs both a continuousflow and a pulsatile flow pump connected in parallel or in series andoperating simultaneously or in an alternating fashion. Yet anotheralternative embodiment employs a rotary pump that is controllable in asynchronous copulsating or counterpulsating fashion, or in someout-of-phase intermediate thereof.

In yet another embodiment, utilizing the benefits of a single siteapplication, the extracardiac system comprises a first conduitcomprising more specifically a biocompatible vascular conduit orvascular graft capable of being applied to a blood vessel via ananastomosis connection or some other mechanical connection usingbiological or synthetic materials. The vascular graft conduit may beentirely synthetic or partially synthetic, with a part intended forintracorporeal use being made with biological material. As with many ofthe other embodiments described herein, this embodiment may be partiallyor fully implantable. In the latter instance, the first conduit could becomprised entirely of biological material, as it would be positionedentirely intracorporeally, although it need not be. The first conduit iscoupled to a pump designed to pump primarily at subcardiac rates, asdescribed further herein, which is then coupled to a second conduit.Unique to this particular embodiment is an arrangement in which thefirst conduit is configured to permit the second conduit to pass throughthe first conduit wall to form an internal lumen between the point ofwall penetration and the blood vessel to which the first and secondconduit penetrate. The wall penetration may comprise simply a hole inthe wall through which the second conduit may pass and to which thesecond conduit may be sealably secured (to prevent leakage).Alternatively, the wall penetration may comprise a branched conduit withan end that permits the second conduit to pass through and be sealablyconnected.

It is contemplated that, where the entire system of the presentinvention is implanted, that it be implanted subcutaneously without theneed for major invasive surgery and, preferably, extrathoracically. Forexample, the pump may be implanted in the groin area, with the inflowconduit attached to the femoral or iliac artery proximate thereto andthe outflow conduit attached to the axillary artery proximate theshoulder. It is contemplated that the outflow conduit be applied bytunneling it under the skin from the pump to the axillary artery.Alternatively, the pump and conduits may be applied intravascularlythrough a non-primary blood vessel in a subcutaneous application. Insuch an embodiment, the pump is sized and configured to be positionedwithin or pass through a non-primary vessel and introduced via apercutaneous insertion or a surgical cutdown with or withoutaccompanying inflow and outflow conduits. The pump may be enclosedwithin a conduit through which blood may be directed, an open housinghaving a cage-like arrangement to shield the pump blades from damagingthe endothelial lining, or a closed housing having an inlet and outletto which inflow and outflow conduits may be respectively attached.

Where implanted, the pump is preferably powered by an implantable powersource, such as for example a battery, that may be regeneratedexternally by an RF induction system or be replaced periodically, and/ora self-generating power source that, for example, draws energy from thehuman body (e. g., muscles, chemicals, heat). The pump may alternativelybe powered by a rotatably driven cable extending and controlledextracorporeally.

The present invention also comprises a method for supplementing thecirculation of blood in the patient and potentially reducing theworkload on the heart of a patient without connecting any component tothe patient's heart. The inventive method comprises the steps of using apump configured to generate blood flow at volumetric rates that are onaverage subcardiac, wherein the pump, whether implantable or not, mayhave an inflow and outflow conduit attached thereto and may be enclosedin an open or closed housing; fluidly coupling a distal end of theinflow conduit to a first peripheral or non-primary blood vessel with aminimally-invasive surgical procedure to permit the flow of blood to thepump from the first peripheral or non-primary blood vessel of thepatient; implanting the inflow conduit subcutaneously; fluidly couplinga distal end of the outflow conduit to a second or same blood vessel,whether primary or non-primary, with a minimally-invasive surgicalprocedure to permit the flow of blood away from the pump to the secondblood vessel of the patient; and operating said pump to perfuse bloodthrough the patient's circulatory system. Equally valuable, the methodcould also involve withdrawing blood from a primary blood vessel anddischarging the blood into a non-primary blood vessel. “Fluid coupling”to a primary vessel referred to herein refers to positioning the distalend of an inflow or outflow conduit within a desired primary vessel forwithdraw or discharge of blood therein. Fluid coupling to a non-primaryvessel referred to herein refers to one of either positioning the distalend of a conduit within the desired blood vessel, applying a catheterpercutaneously or through surgical cut-down, or connecting the conduitto the vessel via an anastomosis procedure or other connection, wherethe conduit functions as a graft. Where the desired peripheral ornon-primary blood vessel is the axillary artery, the step of connectingthe distal end of the outflow conduit may be performed in such a mannerthat a sufficient flow of blood is directed toward the hand to avoidlimb ischemia while ensuring that sufficient flow is directed toward theaorta without damaging the endothelial lining of the axillary vessel.The same concerns for avoiding limb ischemia and damage to theendothelial lining would apply, however, regardless of the selection ofsecond peripheral or non-primary blood vessel.

In one specific application, the pump is capable of synchronous controlwherein the step of operating the pump includes the steps of beginningdischarge of blood out of the pump during isovolumic contraction anddiscontinuing discharge of blood when the aortic valve closes followingsystole. Depending upon the patient and the specific arrangement of thepresent system, this specific method results in reduced afterload and/orpreload on the heart while also supplementing circulation. For example,in one application, the first and second blood vessels are the femoraland axillary arteries, respectively; or the femoral artery and theaorta, respectively. Numerous other combinations may be equallyeffective to achieve the benefits of the present invention.

In an alternative method of applying the present invention, the pump isnot implanted and the inflow and outflow conduits are fluidly coupled tothe first and second blood vessels percutaneously, using areadily-removable connector, such as a cannula, to connect the distalends of each conduit to the blood vessels.

The present invention further comprises a method that comprises thesteps of applying a proximal end of a vascular graft first conduit to apump and a distal end of the first conduit to a non-primary blood vesselvia an anastomosis connection or other connection; fluidly coupling asecond conduit, which is connected at a proximal end to the pump,through the vascular graft first conduit to a non-primary blood vesselso as to form a multi-lumen arrangement; and operating the pump to drawblood from one non-primary blood vessel and returning it to the same ordifferent blood vessel at subcardiac rates to supplement bloodperfusion. The step of fluidly coupling the second conduit to anon-primary blood vessel may comprise attaching the second conduit tothe first conduit and to the pump, where the first conduit ispreconfigured to comprise a multi-lumen catheter between the point ofconnection and the distal end of the first conduit, or it may compriseinserting a cannula end of the second conduit through an opening in thewall of the first conduit and passing it through the first conduit andinto the blood vessel to reside in that same blood vessel or a differentblood vessel.

In yet a different application of the present inventive methods, themethod includes the steps of, prior to applying a shape change therapyinvolving a cardiac reshaping device, applying a blood supplementationsystem to the patient that is designed to reduce the size or wall stressof one or both of the ventricles that results in a reduction inventricular loading, including the steps of providing a pump configuredto pump blood at subcardiac rates, providing inflow and outflow conduitsconfigured to fluidly communicate with one or more non-primary bloodvessels, connecting the inflow conduit to a non-primary blood vessel,connecting the outflow conduit to the same or different blood vessel andoperating the subcardiac pump in a manner, as described herein, toreduce the size and/or wall stress (ventricular load). The methodfurther comprises, after sufficient reduction in ventricular load,applying a cardiac reshaping device, such as those referred to herein,or another capable of serving the same or substantially similarfunction.

An important advantage of the present invention is that it utilizes thebenefits of an IABP, without the requirement of extracorporeal equipmentor the need to have a balloon or similar implement partially obstructinga blood vessel. In addition to the benefits of an IABP, it also offersthe benefit of reducing the preload on the heart. The present inventionthus offers simplicity and long-term use.

Another important advantage of the present invention is its potential toenhance mixing of systemic arterial blood, particularly in the aorta,and thereby deliver blood with a higher oxygen-carrying capacity toorgans supplied by arterial side branches off of the aorta. Thisovercomes the problem of blood streaming in the descending aorta thatmay sometimes occur in patients suffering from low cardiac output orother ailments resulting in low blood flow. The lack of mixing of theblood within the descending aorta that may result from blood streamingcould lead to a higher concentration of red blood cells and nutrients inthe central region of the aorta and a decreasing concentration of redblood cells closer to the aortic wall. This could result in lowerhematocrit blood flowing into branch arteries from the aorta. Where itis desired to address the potential problem of blood streaming, a methodof utilizing the present invention may include taking steps to assesscertain parameters of the patient and then to determine the minimumoutput of the pump that ensures turbulent flow in the aorta, therebyenhancing blood mixing. One embodiment of that method includes the stepof determining the Reynolds number and the average Womersley number forthe flow through the descending aorta before and/or after applying thepresent inventive system to the patient and adjusting the pumpaccordingly.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features and advantages of the invention will now bedescribed with reference to the drawings, which are intended toillustrate and not to limit the invention.

FIG. 1 is a schematic view of a cardiac assist device, known as a leftventricular assist device, showing a bypass from the apex of the leftventricle to the aortic arch;

FIG. 2 is a schematic view of a first embodiment of the presentinvention, shown applied to a patient's circulatory system.

FIG. 3 is a schematic view of a second embodiment of the presentinvention, shown applied to a patient's circulatory system.

FIG. 4 is a schematic view of a variation of the first embodiment ofFIG. 2 shown implanted into a patient;

FIG. 5 is a schematic view of a third embodiment of the presentinvention, shown applied to a patient's circulatory system.

FIG. 6 is a schematic view of a fourth embodiment of the presentinvention, shown applied to a patient's circulatory system.

FIG. 7 is a schematic view of an inflow L-shaped connector, showninserted within a blood vessel.

FIG. 8 is a schematic view of a fifth embodiment of the presentinvention employing a multi-lumen catheter for single site applicationto a patient.

FIG. 9 is a schematic view of a sixth embodiment of the presentinvention showing a reservoir and a portable housing for carrying aportion of the invention directly on the patient.

FIG. 10 is a schematic view of a variation of the third embodiment ofFIG. 5, shown applied to a patient's circulatory system.

FIG. 11 is a schematic view of an application of the embodiment of FIG.2 in which the inflow conduit and outflow conduit are applied to thesame non-primary blood vessel.

FIG. 12 is a schematic view of a seventh embodiment of the presentinvention employing an intravascular pump inserted through a non-primaryvessel in which the pump is enclosed in a protective housing withoutinflow and outflow conduits.

FIG. 13 is a schematic view of an eighth embodiment of the presentinvention employing an intravascular pump inserted through a non-primaryvessel in which the pump is housed within a conduit having an inlet andan outlet.

FIG. 14 is a schematic view of a variation of the eighth embodiment ofFIG. 13 in which an additional conduit is shown adjacent the conduithousing the pump, and in which the pump comprises a shaft mountedhelical thread.

FIG. 15 is a schematic view of a ninth embodiment of the presentinvention employing an inflow vascular graft conduit coupled to anon-primary blood vessel and to a pump, and an outflow conduit fluidlycoupled to a blood vessel through the inflow conduit.

FIG. 16 is a schematic view of a variation of the ninth embodiment ofthe present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Turning now to the drawings provided herein, a more detailed descriptionof the embodiments of the present invention is provided below. It shouldbe noted, however, that while some embodiments have all of theadvantages identified herein, other embodiments may only realize somebut not all of the advantages.

The present invention provides a heart assist system that isextracardiac in nature. In other words, the present inventionsupplements blood perfusion, without the need to interface directly withthe heart and aorta. Thus, no major invasive surgery is necessary to usethe present invention. The present invention also lessens thehemodynamic burden or workload on the heart by reducing the pressure atthe aortic root during systole (afterload) and/or reducing leftventricular end diastolic pressure and volume (preload).

With reference to FIG. 2, a first embodiment of the present invention 10is shown applied to a patient 12 having an ailing heart 14 and an aorta16, from which peripheral brachiocephalic blood vessels extend,including the right subclavian 18, the right carotid 20, the leftcarotid 22, and the left axillary 24. Extending from the descendingaorta is another set of peripheral blood vessels, the left and rightfemoral arteries 26, 28.

The first embodiment 10 comprises a pump 32, having an inlet 34 and anoutlet 36 for connection of flexible conduits thereto. The pump 32 ispreferably a rotary pump, either an axial type or a centrifugal type,although other types of pumps may be used, whethercommercially-available or customized. In either case, the pump should besufficiently small to be implanted subcutaneously and preferablyextrathoracically, for example in the groin area of the patient, withoutthe need for major invasive surgery. Because the present invention is anextracardiac system, no valves are necessary. Any inadvertent backflowthrough the pump and/or through the inflow conduit would not harm thepatient.

Regardless of the style or nature chosen, the pump 32 of the presentinvention is sized to generate blood flow at subcardiac volumetricrates, less than about 50% of the flow rate of an average healthy heart,although flow rates above that may be effective. Thus, the pump 32 ofthe present invention is sized and configured to discharge blood atvolumetric flow rates anywhere in the range of 0.1 to 3 liters perminute, depending upon the application desired and/or the degree of needfor heart assist. For example, for a patient experiencing advancedcongestive heart failure, it may be preferable to employ a pump that hasan average subcardiac rate of 2.5 to 3 liters per minute. In otherpatients, particularly those with minimal levels of heart failure, itmay be preferable to employ a pump that has an average subcardiac rateof 0.5 liters per minute or less. In yet other patients it may bepreferable to employ a pump that is a pressure wave generator that usespressure to augment the flow of blood generated by the heart.

In one embodiment, the pump selected is a continuous flow pump so thatblood perfusion through the circulation system is continuous. In analternative embodiment, the pump selected has the capability ofsynchronous actuation; i. e., it may be actuated in a pulsatile mode,either in copulsating or counterpulsating fashion.

For copulsating action, it is contemplated that the pump 32 would beactuated to discharge blood generally during systole, beginningactuation, for example, during isovolumic contraction before the aorticvalve opens or as the aortic valve opens. The pump would be static whilethe aortic valve is closed following systole, ceasing actuation, forexample, when the aortic valve closes.

For counterpulsating actuation, it is contemplated that the pump 32would be actuated generally during diastole, ceasing actuation, forexample, before or during isovolumic contraction. Such an applicationwould permit and/or enhance coronary blood perfusion. In thisapplication, it is contemplated that the pump would be static during thebalance of systole after the aortic valve is opened, to lessen theburden against which the heart must pump. The aortic valve being openencompasses the periods of opening and closing, wherein blood is flowingtherethrough.

It should be recognized that the designations copulsating andcounterpulsating are general identifiers and are not limited to specificpoints in the patient's heart cycle when the pump begins anddiscontinues actuation. Rather, they are intended to generally refer topump actuation in which the pump is actuating, at least in part, duringsystole and diastole, respectively. For example, it is contemplated thatthe pump might be activated to be out of phase from true copulsating orcounterpulsating actuation described herein, and still be synchronous,depending upon the specific needs of the patient or the desired outcome.One might shift actuation of the pump to begin prior to or afterisovolumic contraction or to begin before or after isovolumic expansion.

Furthermore, the pulsatile pump may be actuated to pulsateasynchronously with the patient's heart. Typically, where the patient'sheart is beating irregularly, there may be a desire to pulsate the pumpasynchronously so that the perfusion of blood by the extracardiacpumping system is more regular and, thus, more effective at oxygenatingthe organs. Where the patient's heart beats regularly, but weakly,synchronous pulsation of the extracardiac pump may be preferred.

The pump 32 is driven by a motor 40 and/or other type of drive means andis controlled preferably by a programmable controller 42 that is capableof actuating the pump in pulsatile fashion, where desired, and also ofcontrolling the speed or output of the pump. For synchronous control,the patient's heart would preferably be monitored with an EKG in whichfeedback would be provided the controller 42. The controller 42 ispreferably programmed by the use of external means. This may beaccomplished, for example, using RF telemetry circuits of the typecommonly used within implantable pacemakers and defibrillators. Thecontroller may also be autoregulating to permit automatic regulation ofthe speed, and/or regulation of the synchronous or asynchronouspulsation of the pump, based upon feedback from ambient sensorsmonitoring parameters, such as pressure or the patient's EKG. It is alsocontemplated that a reverse-direction pump be utilized, if desired, inwhich the controller is capable of reversing the direction of either thedrive means or the impellers of the pump. Such a pump might be usedwhere it is desirable to have the option of reversing the direction ofcirculation between two peripheral blood vessels.

Power to the motor 40 and controller 42 may be provided by a powersource 44, such as a battery, that is preferably rechargeable by anexternal induction source (not shown), such as an RF induction coil thatmay be electromagnetically coupled to the battery to induce a chargetherein. Alternative power sources are also possible, including a devicethat draws energy directly from the patient's body; e. g., the patient'smuscles, chemicals or heat. The pump can be temporarily stopped duringrecharging with no appreciable life threatening effect, because thesystem only supplements the heart, rather than substituting for theheart.

While the controller 42 and power source 44 are preferably pre-assembledto the pump 32 and implanted therewith, it is also contemplated that thepump 32 and motor 40 be implanted at one location and the controller 42and power source 44 be implanted in a separate location. In onealternative arrangement, the pump 32 may be driven externally through apercutaneous drive line. In another alternative, the pump, motor andcontroller may be implanted and powered by an extracorporeal powersource. In the latter case, the power source could be attached to theside of the patient to permit fully ambulatory movement.

The inlet 34 of the pump 32 is preferably connected to a flexible inflowconduit 50 and a flexible outflow conduit 52 to direct blood flow fromone peripheral blood vessel to another. The inflow and outflow conduits50, 52 may, for example, be formed from Dacron, Hemashield or Gortexmaterials, although other synthetic materials may be suitable. Theinflow and outflow conduits 50, 52 may also comprise biologic materialsor pseudobiological (hybrid) materials (e. g., biologic tissue supportedon a synthetic scaffold). The inflow and outflow conduits are preferablyconfigured to minimize kinks so blood flow is not meaningfullyinterrupted by normal movements of the patient or compressed easily fromexternal forces. In some cases, the inflow and/or outflow conduits maycome commercially already attached to the pump. Where it is desired toimplant the pump 32 and the conduits 50, 52, it is preferable that theinner diameter of the conduits be less than 25 mm, although diametersslightly larger may be effective.

In one preferred application of the present invention, the firstembodiment is applied in an arterial-arterial fashion; for example, as afemoral-axillary connection, as is shown in FIG. 2. It should beappreciated by one of ordinary skill in the art that an axillary-femoralconnection would also be effective using the embodiments describedherein. Indeed, it should be recognized by one of ordinary skill in theart that the present invention might be applied to any of the peripheralblood vessels in the patient. In an alternative arrangement, as shown inFIG. 11, the first embodiment may be applied so that the inflow conduitand the outflow conduit are applied subcutaneously to the samenon-primary vessel, in any manner described herein.

The inflow conduit 50 has a first proximal end 56 that connects with theinlet 34 of the pump 32 and a second distal end 58 that connects with afirst peripheral blood vessel, which is preferably the left femoralartery 26 of the patient 12, although the right femoral artery or anyother peripheral artery may be acceptable. In one application, theconnection between the inflow conduit 50 and the first blood vessel isvia an end-to-side anastomosis, although a side-to-side anastomosisconnection might be used mid-stream of the conduit where the inflowconduit were connected at its second end to an additional blood vesselor at another location on the same blood vessel (neither shown).

Similarly, the outflow conduit 52 has a first proximal end 62 thatconnects to the outlet 36 of the pump 32 and a second distal end 64 thatconnects with a second peripheral blood vessel, preferably the leftaxillary artery 24 of the patient 12, although the right axillaryartery, or any other peripheral artery, would be acceptable. In oneapplication, the connection between the outflow conduit 52 and thesecond blood vessel is via an end-to-side anastomosis, although aside-to-side anastomosis connection might be used mid-stream of theconduit where the outflow conduit were connected at its second end toyet another blood vessel (not shown) or at another location on the sameblood vessel. Preferably, the outflow conduit is attached to the secondblood vessel at an angle that results in the predominant flow of bloodout of the pump proximally toward the aorta and heart, such as is shownin FIG. 2, while still maintaining sufficient flow distally toward thehand to prevent limb ischemia.

It is preferred that application of the present invention to theperipheral or non-primary blood vessels be accomplished subcutaneously;i.e., at a shallow depth just below the skin or first muscle layer so asto avoid major invasive surgery. It is also preferred that the presentinvention be applied extrathoracically to avoid the need to invade thepatient's chest cavity. Where desired, the entire extracardiac system ofthe present invention 10 may be implanted within the patient 12, eitherextravascularly or intravascularly or a hybrid thereof In the case of anextravascular application, the pump 32 may be implanted, for example,into the groin area, with the inflow conduit 50 fluidly connectedsubcutaneously to, for example, the femoral artery 26 proximate the pump32. The outflow conduit would be tunneled subcutaneously through to, forexample, the left axillary artery 24. In an alternative arrangement, thepump 32 and associated drive and controller could be temporarilyfastened to the exterior skin of the patient, with the inflow andoutflow conduits 50, 52 connected percutaneously. In either case, thepatient may be ambulatory without restriction of tethered lines.

Referring to FIG. 11, an alternative method of using the presentinvention comprises the steps of fluidly coupling the inflow conduit 50,which is fluidly coupled to pump 32, to a patient subcutaneously to anon-primary blood vessel, either via an anastomosis connection orpercutaneously with a cannula 54, fluidly coupling the outflow conduit52 to the same blood vessel in a desired manner described herein,directing blood from the blood vessel through the inflow conduit,through the pump and the outflow conduit into the blood vessel. In theapplication of FIG. 11, the system is positioned at the patient's leftfemoral artery. Specific applications of this alternative method mayfurther comprise positioning the inflow conduit upstream of the outflowconduit, although the reverse arrangement is also contemplated. It isalso contemplated that either the inflow conduit or the outflow conduitmay extend through the non-primary blood vessel to a second blood vessel(e.g., through the left femoral to the aorta proximate the renal branch)so that blood may be directed from the first to the second blood vesselor vice versa.

It is contemplated that, where an anastomosis connection is not desired,a special connector may be used to connect the conduits 50, 52 to theperipheral blood vessels. With reference to FIG. 3, a second embodimentof the present invention is shown, wherein the inflow conduit 50 andoutflow conduit 52 are connected to the peripheral blood vessels viafirst and second connectors 68, 70 each comprising three-openingfittings. In the preferred embodiment, the connectors 68, 70 comprise anintra-vascular, generally-tee-shaped fitting 72 having a proximal end74, a distal end 76, and an angled divergence 78 permitting connectionto the inflow and outflow conduits 50, 52 and the blood vessels. Theproximal and distal ends 74, 76 of the fittings 72 permit connection tothe blood vessel into which the fitting is positioned. The angle ofdivergence 78 of the fittings 72 may be 90 degrees or less in eitherdirection from the axis of flow through the blood vessel, as optimallyselected to generate the needed flow distally toward the hand to preventlimb ischemia, and to insure sufficient flow and pressure toward theaorta to provide the circulatory assistance and workload reductionneeded while minimizing or avoiding endothelial damage to the vessel. Inanother embodiment, the connectors 68, 70 are sleeves (not shown) thatsurround and attach to the outside of the peripheral blood vessel where,within the interior of the sleeve, a port to the blood vessel isprovided to permit blood flow from the conduits 50, 52 when they areconnected to the connectors 68, 70, respectively.

Other types of connectors having other configurations are contemplatedthat may avoid the need for an anastomosis connection or that permitconnection of the conduits to the blood vessels. For example, it iscontemplated that an L-shaped connector be used if it is desired towithdraw blood more predominantly from one direction of a peripheralvessel or to direct blood more predominantly into a peripheral vessel.Referring to FIG. 7, an inflow conduit 50 is fluidly connected to aperipheral vessel, for example, the left femoral artery 26, using anL-shaped connector 310. The connector 310 has an inlet port 312 at aproximal end and an outlet port 314 through which blood flows into theinflow conduit 50. The connector 310 also has an arrangement of holes316 within a wall positioned at a distal end opposite the inlet port 312so that some of the flow drawn into the connector 310 is divertedthrough the holes 312, particularly downstream of the connector, as inthis application. A single hole in the wall could also be effective,depending upon size and placement. The connector may be a deformableL-shaped catheter percutaneously applied to the blood vessel or, in analternative embodiment, be connected directly to the walls of the bloodvessel for more long term application. By directing some blood flowdownstream of the connector during withdrawal of blood from the vessel,ischemic damage downstream from the connector may be avoided. Suchischemic damage might otherwise occur if the majority of the bloodflowing into the inflow connector were diverted from the blood vesselinto the inflow conduit. It is also contemplated that a connection tothe blood vessels might be made via a cannula, wherein the cannula isimplanted, along with the inflow and outflow conduits.

The advantage of discrete connectors is their potential application topatients with chronic CHF. A connector eliminates a need for ananastomosis connection between the conduits of the present inventionsystem and the peripheral blood vessels where it is desired to removeand/or replace the system more than one time. The connectors could beapplied to the first and second blood vessels semi-permanently, with anend cap applied to the divergence for later quick-connection of thepresent invention system to the patient. In this regard, a patient mightexperience the benefit of the present invention periodically, withouthaving to reconnect and redisconnect the conduits from the blood vesselsvia an anastomosis procedure each time. Each time it is desired toimplement the present invention, the end caps would be removed and theconduit attached to the connectors quickly.

In the preferred embodiment of the connector 70, the divergence 78 is.oriented at an acute angle significantly less than 90° from the axis ofthe fitting 72, as shown in FIG. 3, so that a majority of the bloodflowing through the outflow conduit 52 into the blood vessel (e. g.,left axillary 24) flows in a direction proximally toward the heart 14,rather than in the distal direction. In an alternative embodiment, theproximal end 74 of the fitting 72 may have a diameter larger than thediameter of the distal end 76, without need of having an angleddivergence, to achieve the same result.

With or without a connector, with blood flow directed proximally towardthe aorta, the result may be concurrent flow down the descending aorta,which will result in the reduction of pressure at the aortic root. Thus,the present invention may be applied so to reduce the afterload on thepatient's heart, permitting at least partial if not complete CHFrecovery, while supplementing blood circulation. Concurrent flow dependsupon the phase of operation of the pulsatile pump and the choice ofsecond blood vessel to which the outflow conduit is connected.

While the present invention may be applied to create anarterial-arterial flow path, given the nature of the present invention,i. e., supplementation of circulation to meet organ demand, avenous-arterial flow path may also be used. For example, with referenceto FIG. 4, one embodiment of the present invention 10 may be applied tothe patient 12 such that the inflow conduit 50 is connected to aperipheral vein, such as the left femoral vein 80. In this arrangement,the outflow conduit 50 may be connected to one of the peripheralarteries, such as the left axillary 24. Arterial-venous arrangements arecontemplated as well. In those venous-arterial cases where the inflow isconnected to a vein and the outflow is connected to an artery, the pump32 should be sized to permit flow sufficiently small so thatoxygen-deficient blood does not rise to unacceptable levels in thearteries. It should be appreciated that the connections to theperipheral veins could be by one or more methods described above forconnecting to a peripheral artery. It should also be appreciated thatthe present invention could be applied as a venous-venous flow path,wherein the inflow and outflow are connected to separate peripheralveins. In addition, an alternative embodiment comprises two discretepumps and conduit arrangements, one being applied as a venous-venousflow path, and the other as an arterial-arterial flow path. When venousblood is mixed with arterial blood either at the inlet of the pump orthe outlet of the pump the ratio of venous blood to arterial bloodshould be controlled to maintain an arterial saturation of a minimum of80% at the pump inlet or outlet. Arterial saturation can be measuredand/or monitored by pulse oximetry, laser doppler, colorimetry or othermethods used to monitor blood oxygen saturation. The venous blood flowinto the system can then be controlled by regulating the amount of bloodallowed to pass through the conduit from the venous-side connection.

A partial external application of the present invention is contemplatedwhere a patient's heart failure is acute; i. e., is not expected to lastlong, or in the earlier stages of heart failure (where the patient is inNew York Heart Association Classification (NYHAC) functional classes IIor III). With reference to FIGS. 5 and 10, a third embodiment of thepresent invention 110 is applied percutaneously to a patient 112 toconnect two peripheral blood vessels wherein a pump 132 and itsassociated driving means and controls are employed extracorporeally. Thepump 132 has an inflow conduit 150 and an outflow conduit 152 associatedtherewith for connection to two peripheral blood vessels. The inflowconduit 150 has a first end 156 and second end 158 wherein the secondend is connected to a first peripheral blood vessel (e. g., femoralartery 126) by way of a cannula 180. The cannula 180 has a first end 182sealably connected to the second end 158 of the inflow conduit 150. Thecannula 180 also has a second end 184 that is inserted through asurgical opening 186 or an introducer sheath (not shown) and into theblood vessel source (e. g., femoral artery 126).

Similarly, the outflow conduit 152 has a first end 162 and second end164 wherein the second end is connected to a second peripheral bloodvessel (e. g., left axillary artery 124, as shown in FIG. 5, or theright femoral 127, as shown in FIG. 10) by way of a cannula 180. Likethe inflow cannula, the outflow cannula 180 has a first end 182 sealablyconnected to the second end 164 of the outflow conduit 152. The outflowcannula 180 also has a second end 184 that is inserted through surgicalopening 190 or an introducer sheath (not shown) and into the secondblood vessel (e. g., left axillary artery 124 or right femoral 127). Asshown in FIG. 10, the second end 184 of the outflow cannula may extendwell into the aorta, for example, proximal to the left subclavian. Ifdesired, it may also terminate within the left subclavian artery or theleft axillary artery, or it may terminate in the mesenteric or renalarteries (not shown), where in either case, the cannula has passedthrough at least a portion of a primary artery (in this case, theaorta). Also, if desired, blood drawn into the extracardiac systemdescribed herein may originate from the descending aorta (or an arterybranching therefrom) and be directed into a blood vessel that is neitherthe aorta nor pulmonary artery. By use of a percutaneous application,the present invention may be applied temporarily without the need toimplant any aspect thereof or to make anastomosis connections to theblood vessels.

It is contemplated that a means for minimizing the loss of thermalenergy in the patient's blood be provided where the present inventivesystem is applied extracorporeally. Such means for minimizing the lossof thermal energy may comprise, for example, a heated bath through whichthe inflow and outflow conduits pass or, alternatively, thermal elementssecured to the exterior of the inflow and outflow conduits. Referring toFIG. 9, one embodiment comprises an insulating wrap 402 surrounding theoutflow conduit 152 having one or more thermal elements passingtherethrough. The elements may be powered, for example, by a battery(not shown). One advantage of thermal elements is that the patient maybe ambulatory, if desired. Other means that are known by persons ofordinary skill in the art for ensuring that the temperature of thepatient's blood remains at acceptable levels while travellingextracorporeally are also contemplated.

An alternative variation of the third embodiment may be used where it isdesired to treat a patient periodically, but for short periods of timeeach occasion and without the use of special connectors. With thisvariation, it is contemplated that the second ends of the inflow andoutflow conduits be more permanently connected to the associated bloodvessels via, for example, an anastomosis connection, wherein a portionof each conduit proximate to the blood vessel connection is implantedpercutaneously with a removable cap enclosing the externally-exposedfirst end (or an intervening end thereof) of the conduit external to thepatient. When it is desired to provide a circulatory flow path tosupplement blood flow, the removable cap on each exposedpercutaneously-positioned conduit could be removed and the pump (or thepump with a length of inflow and/or outflow conduit attached thereto)inserted between the exposed percutaneous conduits. In this regard, apatient may experience the benefit of the present inventionperiodically, without having to reconnect and redisconnect the conduitsfrom the blood vessels each time.

Another embodiment of the present invention includes a plurality ofinflow and/or outflow conduits. For example, with reference to FIG. 6, afourth embodiment of the present invention 210 includes a pump 232 influid communication with a plurality of inflow conduits 250A, 250B and aplurality of outflow conduits 252A, 252B. Each pair of conduitsconverges at a generally Y-shaped convergence 296 that converges theflow at the inflow end and diverges the flow at the outflow end. Eachconduit may be connected to a separate peripheral blood vessel, althoughit is possible to have two connections to the same blood vessel atremote locations. In one arrangement, all four conduits are connected toperipheral arteries. Alternatively, one or more of the conduits could beconnected to veins. In the application shown in FIG. 6, inflow conduit250A is connected to left femoral artery 226 while inflow conduit 250Bis connected to left femoral vein 278. Outflow conduit 252A is connectedto left axillary artery 224 while outflow conduit 252B is connected toleft carotid artery 222. It should be noted that the connections of anyor all of the conduits to the blood vessels may be via an anastomosisconnection or via a special connector, as described above. In addition,the embodiment of FIG. 6 may be applied to any combination of peripheralblood vessels that would best suit the patient's condition. For example,it may be desired to have one inflow conduit and two outflow conduits orvice versa. It should be noted that more than two conduits may be usedon the inflow or outflow side, where the number of inflow conduits isnot necessarily equal to the number of outflow conduits.

If desired, the present inventive system may further comprise areservoir that is either contained within or in fluid communication withthe inflow conduit. This reservoir is preferably made of materials thatare nonthrombogenic. Referring to FIG. 9, a reservoir 420 is positionedfluidly in line with the inflow conduit 150. The reservoir 420 serves tosustain adequate blood in the system when the pump demand exceedsmomentarily the volume of blood available in the peripheral blood vesselin which the inflow conduit resides until the pump output can beadjusted. The reservoir reduces the risk of excessive drainage of bloodfrom the peripheral blood vessel, which may occur when cardiac outputfalls farther than the already diminished baseline level of cardiacoutput, or when there is systemic vasodilation, as can occur, forexample, with septic shock. It is contemplated that the reservoir wouldbe primed with an acceptable solution, such as saline, when the presentsystem is first applied to the patient.

In an alternative embodiment, the present system comprises a multi-lumencatheter whereby the system may be applied by insertion at a singlecannulated site while the inflow and outflow conduits still fluidlycommunicate with peripheral vessels. Referring to FIG. 8, a multi-lumencatheter 510 could be inserted, for example, into the left femoralartery 26 and guided superiorly through the descending aorta to one ofnumerous locations. The blood could discharge, for example, directlyinto the descending aorta proximate an arterial branch, such as the leftsubclavian artery or, as shown in FIG. 2 by way of example, directlyinto the peripheral mesenteric artery 30. Preferably, the multi-lumencatheter 510 has an inflow port 512 that may be positioned within theleft femoral artery 26 when the catheter 510 is fully inserted so thatblood drawn from the left femoral artery is directed through the inflowport 512 into a first lumen 514 in the catheter. This blood is thenpumped through a second lumen 516 in the catheter and out through anoutflow port 520 at the distal end of the catheter 510. The outflow port520 may be situated within, for example, the mesenteric artery 30 suchthat blood flow results from the left femoral artery 26 to themesenteric artery 30. Preferably, where there is a desire for thepatient to be ambulatory, the multi-lumen catheter 510 should preferablybe made of material sufficiently flexible and resilient to permit thepatient to be comfortably move about while the catheter is indwelling inthe patient's blood vessels without causing any vascular trauma.

As explained above for several embodiments, one of the advantages of thepresent heart assist system is that it permits the patient to beambulatory. If desired, the system may be designed portably so that itmay be carried directly on the patient. Referring to FIG. 9, this may beaccomplished through the use of a portable case 610 with a belt strap612 to house the pump, power supply and/or the controller, along withcertain portions of the inflow and/or outflow conduits, if necessary. Itmay also be accomplished with a shoulder strap or other techniques, suchas a backpack or a fanny pack, that permit effective portability. Asshown in FIG. 9, blood is drawn through the inflow conduit 150 into apump contained within the portable case 610, where it is discharged intothe outflow conduit 152 back into the patient.

An alternative embodiment of the present invention takes furtheradvantage of the supplemental blood perfusion and heart load reductionbenefits while remaining minimally invasive in application.Specifically, it is contemplated to provide an extracardiac pumpingsystem that comprises a pump that is sized and configured to beimplanted intravascularly in any location desirable to achieve thosebenefits, while being insertable through a non-primary vessel. Referringto FIG. 12, one intrasvascular embodiment 710 of the present inventionis intended for use within a patient's vasculature, as shown, andcomprises a pumping means 712 comprising preferably one or morerotatable impeller blades 714, although other types of pumping means arecontemplated, such as an archimedes screw, a worm pump, or other meansby which blood may be directed axially along the pumping means from apoint upstream of an inlet to the pumping means to a point downstream ofan outlet from the pumping means. Where one or more impellers are used,such as a rotary pump, such impellers may be supported helically orotherwise on a shaft 716 within a housing 720. The housing 720 may beopen, as shown, in which the walls of the housing are open to blood flowtherethrough. The housing, if desired, may be entirely closed except foran inlet and outlet (not shown) to permit blood flow therethrough in amore channel fashion. In either case, the invention serves to supplementthe kinetic energy of the blood flow through the blood vessel in whichthe pump is positioned.

The pump impeller blade(s) 714 of this embodiment may be driven in oneor a number of ways known to persons of ordinary skill in the art. Inthe embodiment shown in FIG. 12, the pump impeller is drivenmechanically via a rotatable cable or drive wire 722 by driving means724, the latter of which may be positioned corporeally (within orwithout the vasculature) or extracorporeally. As shown, the drivingmeans 724 may comprise a motor 726 to which energy is supplied directlyvia an associated battery or an external power source, in a mannerdescribed in more detail herein. It is also contemplated that the pumpbe driven electromagnetically through an internal or externalelectromagnetic drive. Preferably, a controller (not shown) is providedin association with this embodiment so that the pump may be controlledto operate in a continuous and/or pulsatile fashion, as describedherein.

Variations of the intravascular embodiment of FIG. 12 are shown in FIGS.13 and 14. In the embodiment of FIG. 13, the present invention consistsof an intrasvascular extracardiac system 810 comprising a pumping means812, which may be one of several means described herein, whereby thepump means may be driven by one of several pumping means describedherein, including means that is sized and configured to be implantableand, if desired, implantable intravascularly. For a blood vessel (e.g.,descending aorta) having a diameter “A”, the pumping means preferablyhas a meaningfully smaller diameter “B”. The pumping means 812 maycomprise a pump 814 having an inlet 816 and outlet 820 housed within aconduit 822, or may comprise a pump and inflow and outflow conduits (notshown) fluidly connected to the inlet and outlets of pump 814,respectively. The conduit 822 may be relatively short, as shown, or mayextend well within the designated blood vessel or even into an adjoiningor remote blood vessel at either the inlet end, the outlet end, or both.In an alternative embodiment, an intrasvascular pumping means may bepositioned within one lumen of a multilumen catheter so that, forexample, where the catheter is applied at the left femoral artery, afirst lumen may extend into the aorta proximate the left subclavian andthe pumping means may reside at any point within the first lumen, andthe second lumen may extend much shorter just into the left femoral orleft iliac.

In the case of the pumping means of FIG. 13, the means comprises arotary pump driven mechanically by a drive. Referring to FIG. 14, theintravascular extracardiac system may further comprise an additionalconduit 830 positioned preferably proximate the pumping means 812 toprovide a defined flow path for blood flow axially parallel to the bloodflowing through the pumping means. In the case of the pumping means ofFIG. 14, the means comprises a rotatable cable 834 having blooddirecting means 836 supported therein for directing blood axially alongthe cable. Other types of pumping means are also contemplated, ifdesired, for use with the additional conduit 830.

The intravascular extracardiac system described herein may be insertedinto a patient's vasculature in any means known by one of ordinary skillor obvious variant thereof. In one method of use, the system istemporarily housed within a catheter that is inserted percutaneously, orby surgical cutdown into a non-primary blood vessel and fed through to adesired location. The catheter may be withdrawn away from the system soas not to interfere with operation of the system, but still permit thewithdrawal of the system from the patient when desired.

Another alternative embodiment of the present invention takes furtheradvantage of the supplemental blood perfusion and heart load reductionbenefits while remaining minimally invasive in application. Referring toFIG. 15, an extracardiac pumping system 900 comprises a pump 910, aninflow conduit comprising a vascular graft 912, and an outflow conduit914, wherein each of the vascular graft conduit 912 and the outflowconduit 914 are fluidly coupled to pump 910. The pump 910 is configuredto pump blood through the patient at subcardiac volumetric rates, andhas an average flow rate that, during normal operation thereof, issubstantially below that of the patient's heart when healthy. In onevariation, the pump 910 may be a rotary pump. Other pumps describedherein, or any other suitable pump can also be used in the extracardiacpumping system 900. In one application, the pump 910 is configured so asto be implantable.

The vascular graft 912 has a first distal end 916 and a second proximalend 918. The first end 916 is sized and configured to couple to anon-primary blood vessel 920 subcutaneously to permit application of theextracardiac pumping system 900 in a minimally-invasive procedure. Inone application, the vascular graft conduit is configured to couple tothe blood vessel via an anastomosis connection. The second end 918 ofthe vascular graft 912 is fluidly coupled to the pump 910 to conductblood between the non-primary blood vessel 920 and the pump 910. In theembodiment shown, the second end 918 is directly connected to the pump910, but, as discussed above in connection with other embodiments,intervening fluid conducting elements may be interposed between thesecond end 918 of the vascular graft 912 and the pump 910. Examples ofarrangements of vascular graft conduits may be found in U.S. applicationSer. No. 09/780,083, filed Feb. 9, 2001, entitled EXTRA-CORPOREALVASCULAR CONDUIT, which is hereby incorporated by reference in itsentirety and made a part of this specification.

FIG. 15 illustrates that the present inventive embodiment furthercomprises means for connecting the outflow conduit to the vascular graft912, which may comprise in one embodiment an insertion site 922. In theillustrated embodiment, the insertion site is located between the firstend 916 and the second end 918 of the vascular graft 912. The insertionsite 922 is configured to receive the outflow conduit 914 therethroughin a sealable manner. The outflow conduit 914 has a first distal end 924sized and configured as a cannula 928 to be inserted through thenon-primary blood vessel 920 through the vascular graft 912. The conduithas a second proximal end 926 fluidly coupled to the pump 910 to conductblood between the pump 910 and the patient.

The extracardiac pumping system 900 can be applied to a patient, asshown in FIG. 15, so that the outflow conduit 914 provides fluidcommunication between the pump 910 and a location upstream or downstreamof the point where the cannula 928 of the outflow conduit enters thenon-primary blood vessel 920. In another application, the cannula 928 isdirected through the blood vessel to a different blood vessel, upstreamor downstream thereof. Although the vascular graft 912 is describedabove as an “inflow conduit” and the conduit 914 is described above asan “outflow conduit,” in another aspect of this embodiment, the bloodflow through the pumping system 900 is reversed (i.e., the pump 910pumps blood in the opposite direction), whereby the vascular graft 912is an outflow conduit and the conduit 914 is an inflow conduit.

A variation of the extracardiac pumping system in FIG. 15 is shown inFIG. 16. Extracardiac pumping system 950 is similar to the extracardiacpumping system 900 and includes a vascular graft 952 that comprises thefirst end 916, the second end 918, and means for connecting the outflowconduit 914 to the vascular graft 952. The means for connecting theconduit 914 to the vascular graft 952 may comprise a branched portion954. In one embodiment, the branched portion 954 is located between thefirst end 916 and the second end 918. The branched portion 954 isconfigured to sealably receive the distal end of outflow conduit 914.Where, as shown, the first end 924 of the outflow conduit 914 comprisesthe cannula 928, the branched portion 954 is configured to receive thecannula 928. The inflow conduit 952 of this arrangement comprises inpart a multi-lumen catheter, where the internal lumen extends into theblood vessel 920. Examples of such an arrangement of a multi-lumencatheter are shown in U.S. application Ser. No. 10/078,283, filed Feb.14, 2002, entitled A MULTILUMEN CATHETER FOR MINIMIZING LIMB ISCHEMIA,which is hereby incorporated by reference in its entirety and made apart of this specification.

An important advantage of the present invention is its potential toenhance mixing of systemic arterial blood, particularly in the aorta.Such enhanced mixing ensures the delivery of blood with higheroxygen-carrying capacity to organs supplied by arterial side branchesoff of the aorta. A method of enhancing mixing utilizing the presentinvention preferably includes taking steps to assess certain parametersof the patient and then to determine the minimum output of the pumpthat, when combined with the heart output, ensures turbulent flow in theaorta, thereby enhancing blood mixing.

Blood flow in the aortic arch during normal cardiac output may becharacterized as turbulent in the end systolic phase. It is known thatturbulence in a flow of fluid through pipes and vessels enhances theuniform distribution of particles within the fluid. It is believed thatturbulence in the descending aorta enhances the homogeneity of bloodcell distribution in the aorta. It is also known that laminar flow ofviscous fluids leads to a higher concentration of particulates in thecentral portion of pipes and vessels through which the fluid flows. Itis believed that, in low flow states such as that experienced duringheart failure, there is reduced or inadequate mixing of blood cellsleading to a lower concentration of nutrients at the branches of theaorta to peripheral organs and tissues. As a result, the blood flowinginto branch arteries off of the aorta will likely have a lowerhematocrit, especially that flowing into the renal arteries, the celiactrunk, the spinal arteries, and the superior and inferior mesentericarteries. That is because these branches draw from the periphery of theaorta The net effect of this phenomenon is that the blood flowing intothese branch arteries has a lower oxygen-carrying capacity, becauseoxygen-carrying capacity is directly proportional to both hematocrit andthe fractional O₂ saturation of hemoglobin. Under those circumstances,ii is very possible that these organs will experience ischemia-relatedpathology.

The phenomenon of blood streaming in the aorta, and the resultantinadequate mixing of blood resulting in central lumenal concentration ofblood cells, is believed to occur when the Reynolds number (N_(R)) forthe blood flow in the aorta is below 2300. To help ensure that adequatemixing of blood will occur in the aorta to prevent blood cells fromconcentrating in the center of the lumen, a method of applying thepresent invention to a patient may also include steps to adjust theoutput of the pump to attain turbulent flow within the descending aortaupstream of the organ branches; i.e., flow exhibiting a peak Reynoldsnumber of at least 2300 within a complete cycle of systole and diastole.Because flow through a patient is pulsatile in nature, and notcontinuous, consideration must be given to how frequently the blood flowthrough the aorta has reached a certain desired velocity and, thus, adesired Reynolds number. The method contemplated herein, therefore,should also include the step of calculating the average Womersley number(N_(W)), which is a function of the frequency of the patient's heartbeat. It is desired that a peak Reynolds number of at least 2300 isattained when the corresponding Womersley number for the same blood flowis approximately 6 or above.

More specifically, the method may comprise calculating the Reynoldsnumber for the blood flow in the descending aorta by determining theblood vessel diameter and both the velocity and viscosity of the fluidflowing through the aorta. The Reynolds number may be calculatedpursuant to the following equation:

$N_{R} = \frac{V \cdot d}{\upsilon}$where: V=the velocity of the fluid; d=the diameter of the vessel; andυ=the viscosity of the fluid. The velocity of the blood flowing throughthe aorta is a function of the cross-sectional area of the aorta and thevolume of flow therethrough, the latter of which is contributed both bythe patient's own cardiac output and by the output of the pump of thepresent invention. Velocity may be calculated by the following equation:

$V = \frac{Q}{\pi\; r^{2}}$where Q=the volume of blood flowing through the blood vessel per unittime, e. g., the aorta, and r=radius of the aorta. If the relationshipbetween the pump output and the velocity is already known orindependently determinable, the volume of blood flow Q may consist onlyof the patient's cardiac output, with the knowledge that that outputwill be supplemented by the subcardiac pump that is part of the presentinvention. If desired, however, the present system can be implementedand applied to the patient first, before calculating Q, which wouldconsist of the combination of cardiac output and the pump output.

The Womersley number may be calculated as follows:N _(W) =r√{square root over (2πω/υ)}where r is the radius of the vessel being assessed, cw is the frequencyof the patient's heartbeat, and υ=the viscosity of the fluid. For a peakReynolds number of at least 2300, a Womersley number of at least 6 ispreferred, although a value as low as 5 would be acceptable.

By determining (i) the viscosity of the patient's blood, which isnormally about 3.0 mm²/sec (kinematic viscosity), (ii) the cardiacoutput of the patient, which of course varies depending upon the levelof CHF, and (iii) the diameter of the patient's descending aorta, whichvaries from patient to patient but is about 21 mm for an average adult,one can determine the flow rate Q that would result in a velocitythrough the aorta necessary to attain a Reynolds number of at least 2300at its peak during the patient's heart cycle. Based upon thatdetermination of Q, one may adjust the output of the pump of the presentinvention to attain the desired turbulent flow characteristic throughthe aorta, enhancing mixing of the blood therethrough.

One may use ultrasound (e. g., echocardiography or abdominal ultrasound)to measure the diameter of the aorta, which is relatively uniform indiameter from its root to the abdominal portion of the descending aorta.Furthermore, one may measure cardiac output using a thermodilutioncatheter or other techniques known to those of skill in the art.Finally, one may measure viscosity of the patient's blood by using knownmethods; for example, using a capillary viscosimeter. It is expectedthat in many cases, the application of this embodiment of the presentmethod will provide a basis to more finely tune the system to moreoptimally operate the system to the patient's benefit. Other methodscontemplated by the present invention may include steps to assess otherpatient parameters that enable a person of ordinary skill in the art tooptimize the present system to ensure adequate mixing within thevascular system of the patient.

Alternative inventive methods that provide the benefits discussed hereininclude the steps of, prior to applying a shape change therapy, applyinga blood supplementation system (such as one of the many examplesdescribed herein) to a patient, whereby the methods are designed toimprove the ability to reduce the size and/or wall stress of the leftventricle, or both ventricles, thus reducing ventricular loading.Specifically, one example of such a method comprises the steps ofproviding a pump configured to pump blood at subcardiac rates, providinginflow and outflow conduits configured to fluidly communicate withnon-primary blood vessels, fluidly coupling the inflow conduit to anon-primary blood vessel, fluidly coupling the outflow conduit to thesame or different (primary or non-primary) blood vessel and operatingthe subcardiac pump in a manner, as described herein, to reduce the loadon the heart, wherein the fluidly coupling steps may comprisesanastomosis, percutaneous cannulazation, positioning the distal end ofone or both conduits within the desired terminal blood vessel or anycombination thereof. The method further comprises, after sufficientreduction in ventricular loading, applying a shape change therapy in theform of, for example, a cardiac reshaping device, such as those referredto herein, or others serving the same or similar function, for thepurpose of further reducing the size of and/or wall stress on one ormore ventricles and, thus, the heart, and/or for the purpose ofmaintaining the patient's heart at a size sufficient to enhance recoveryof the patient's heart.

While the above description has explained the inventive features of theinvention as applied to various embodiments, it will be understood thatthe variations in the form and details of the apparatus or method may bemade by those of ordinary skill in the art without departing from thespirit of the invention. The scope of the invention is indicated by theappended claims herein, however, not by the foregoing description.

1. An extracardiac pumping system for supplementing blood circulationthrough a patient without any component thereof being connected to thepatient's heart, the extracardiac system comprising: a pump configuredto pump blood through the patient at subcardiac volumetric rates, saidpump having an average flow rate that, during normal operation thereof,is substantially below that of the patient's heart when healthy; a firstconduit having a first distal end sized and configured to fluidly coupleto a non-primary blood vessel, the first conduit also being fluidlycoupled to the pump to conduct blood between the pump and thenon-primary blood vessel; and a second conduit having a first distal endsized and configured to be positioned at least in part within thenon-primary blood vessel and within the first conduit, the secondconduit being fluidly coupled to the pump to conduct blood between thepump and the patient, the first conduit configured to permit the secondconduit to sealably extend through a wall of said first conduit to forman internal lumen within the conduit; whereby the first conduit may befluidly coupled to the blood vessel subcutaneously to permit applicationof the extracardiac pumping system in a minimally-invasive procedurethrough a single site.
 2. The extracardiac pumping system of claim 1,wherein the first conduit is configured as an inflow conduit and thesecond conduit is configured as an outflow conduit.
 3. The extracardiacpumping system of claim 1, wherein the first conduit is configured as anoutflow conduit and the second conduit is configured as an inflowconduit.
 4. The extracardiac pumping system of claim 1, wherein thefirst conduit comprises an insertion site in said first conduit wallsized to tightly fit over the exterior wall of the second conduitextending therethrough and configured to permit a reliable seal betweenthe first conduit wall and the exterior of the second conduit.
 5. Theextracardiac pumping system of claim 4, further comprising a branchedportion on the first conduit located between the first and second end ofsaid first conduit, the insertion site being positioned on said branchedportion.
 6. The extracardiac pumping system of claim 1, wherein thefirst conduit comprises a connector extending from said first conduitconfigured to sealably connect to a distal end of said second conduit;the first conduit further comprising an internal lumen in sealed fluidcommunication with said connector to permit fluid communication betweenthe second conduit and the internal lumen when the distal end of thesecond conduit is connected to the connector without said fluid residingin said second conduit significantly leaking into the first conduit. 7.The extracardiac pumping system of claim 1, wherein the pump is a rotarypump.
 8. The extracardiac pumping system of claim 1, wherein the pump isimplantable.
 9. The extracardiac pumping system of claim 1, wherein thesystem is implantable.
 10. The extracardiac pumping system of claim 1,wherein the first conduit is configured to couple to the blood vesselvia an anastomosis procedure.
 11. A method for treating a patientcomprising: connecting a first end of a first conduit to a first bloodvessel using a minimally invasive procedure to permit the flow of bloodbetween a pump and the first blood vessel,; fluidly coupling a distalend of a second conduit, which is fluidly coupled to the pump at aproximal end, to the patient's vasculature through the first conduit andthrough at least a part of the first blood vessel ;and operating thepump to perfuse blood through the patient's circulatory system atvolumetric rates that are on average subcardiac between the first bloodvessel and the same or different blood vessel.
 12. The method of claim11, wherein the step of fluidly coupling a distal end of the secondconduit to the patient's vasculature comprises directing the distal endof the second conduit through an insertion site positioned on said firstconduit.
 13. The method of claim 11, wherein the step of fluidlycoupling a distal end of the second conduit to the patient's vasculaturecomprises connecting the distal end of the second conduit to a connectorextending from said first conduit.
 14. The extracardiac pumping systemof claim 11, wherein the first conduit is configured to couple to theblood vessel via an anastomosis procedure.